Literature DB >> 7744078

Site-directed mutagenesis of His343-->Ala in Citrobacter freundii tyrosine phenol-lyase. Effects on the kinetic mechanism and rate-determining step.

H Chen1, P Gollnick, R S Phillips.   

Abstract

His343 in Citrobacter freundii tyrosine phenol-lyase is conserved in all known sequences of both tyrosine phenol-lyase and tryptophan indole-lyase; it is located near the active-site Lys257 in C. freundii tyrosine phenol-lyase [Antson, A. A., Demidkina, T. V., Gollnick, P., Danter, Z., Von Tersch, R.L., Long, J., Berezhnoy, S. N., Phillips, R. S., Harutyunyan, E. H. & Wilson, K. S. (1993) Biochemistry 32, 4195--4206]. In order to evaluate the role of His343 in the reaction mechanism of tyrosine phenol-lyase and tryptophan indole-lyase, we have mutated it to Ala; the former mutant is referred to as [H343A]tyrosine phenol lyase. All substrates for alpha, beta-elimination (except S-ethyl-L-cysteine) exhibited lower kcat (10-30%) and kcat/Km (1-10%) values with [H343A]tyrosine phenol-lyase than with the wild-type enzyme. The mutant also shows slower rates of deuterium isotope exchange for L-phenylalanine and L-methionine than does the wild type. The pH-dependent behavior in the reaction of 3-fluoro-L-tyrosine with wild-type tyrosine phenol-lyase is identical to that of L-tyrosine described previously [Kiick, D. M. & Phillips, R. S. (1988) Biochemistry 27, 7333-7338]. The pH profile of kcat/Km for this reaction exhibits two pKa values with an average of 7.7 +/- 0.2, indicating that the catalytic mechanism requires two essential basic groups. The pH profile of kcat/Km for 3-fluoro-L-tyrosine with [H343A]tyrosine phenol-lyase also exhibits two pKa values with an average of 7.8 +/- 0.3. However, kcat for 3-fluoro-L-tyrosine is pH-dependent for the mutant, exhibiting two pKa values with an average of about 7.8, whereas it is pH-independent for the wild type. Steady-state kinetic isotope effects on the reactions with wild-type and [H343A]tyrosine phenol-lyase were examined at various pH values. For the wild type, the values of the isotope effects on kcat and kcat/Km for 3-fluoro-L-[alpha-2H]-tyrosine are independent of pH and equal to 3.9 +/- 0.2 and 2.2 +/- 0.3, respectively, while the corresponding values for [H343A]tyrosine phenol-lyase are 5.4 +/- 0.2 and 3.8 +/- 0.3, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7744078

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  15 in total

1.  Tyrosine phenol-lyase: the role of the coenzyme-binding residue Ser-254 in catalysis.

Authors:  A I Papisova; N P Bazhulina; N G Faleev; T V Demidkina
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2.  Charge-Transfer Dynamics at the α/β Subunit Interface of a Photochemical Ribonucleotide Reductase.

Authors:  Lisa Olshansky; JoAnne Stubbe; Daniel G Nocera
Journal:  J Am Chem Soc       Date:  2016-01-21       Impact factor: 15.419

3.  Glutamate 350 Plays an Essential Role in Conformational Gating of Long-Range Radical Transport in Escherichia coli Class Ia Ribonucleotide Reductase.

Authors:  Kanchana Ravichandran; Ellen C Minnihan; Qinghui Lin; Kenichi Yokoyama; Alexander T Taguchi; Jimin Shao; Daniel G Nocera; JoAnne Stubbe
Journal:  Biochemistry       Date:  2017-02-02       Impact factor: 3.162

4.  Formal Reduction Potentials of Difluorotyrosine and Trifluorotyrosine Protein Residues: Defining the Thermodynamics of Multistep Radical Transfer.

Authors:  Kanchana R Ravichandran; Allan B Zong; Alexander T Taguchi; Daniel G Nocera; JoAnne Stubbe; Cecilia Tommos
Journal:  J Am Chem Soc       Date:  2017-02-21       Impact factor: 15.419

5.  Threonine-124 and phenylalanine-448 in Citrobacter freundii tyrosine phenol-lyase are necessary for activity with L-tyrosine.

Authors:  Tatyana V Demidkina; Maria V Barbolina; Nicolai G Faleev; Bakthavatsalam Sundararaju; Paul D Gollnick; Robert S Phillips
Journal:  Biochem J       Date:  2002-05-01       Impact factor: 3.857

6.  C-S bond cleavage by a polyketide synthase domain.

Authors:  Ming Ma; Jeremy R Lohman; Tao Liu; Ben Shen
Journal:  Proc Natl Acad Sci U S A       Date:  2015-08-03       Impact factor: 11.205

7.  Tyrosine phenol-lyase and tryptophan indole-lyase encapsulated in wet nanoporous silica gels: Selective stabilization of tertiary conformations.

Authors:  Barbara Pioselli; Stefano Bettati; Tatyana V Demidkina; Lyudmila N Zakomirdina; Robert S Phillips; Andrea Mozzarelli
Journal:  Protein Sci       Date:  2004-04       Impact factor: 6.725

8.  Formal reduction potential of 3,5-difluorotyrosine in a structured protein: insight into multistep radical transfer.

Authors:  Kanchana R Ravichandran; Li Liang; JoAnne Stubbe; Cecilia Tommos
Journal:  Biochemistry       Date:  2013-11-22       Impact factor: 3.162

9.  Crystallographic snapshots of tyrosine phenol-lyase show that substrate strain plays a role in C-C bond cleavage.

Authors:  Dalibor Milić; Tatyana V Demidkina; Nicolai G Faleev; Robert S Phillips; Dubravka Matković-Čalogović; Alfred A Antson
Journal:  J Am Chem Soc       Date:  2011-09-27       Impact factor: 15.419

10.  Insights into the catalytic mechanism of tyrosine phenol-lyase from X-ray structures of quinonoid intermediates.

Authors:  Dalibor Milić; Tatyana V Demidkina; Nicolai G Faleev; Dubravka Matković-Calogović; Alfred A Antson
Journal:  J Biol Chem       Date:  2008-08-20       Impact factor: 5.157

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